Reactions of Epoxides Prepared from Some Monoterpenes with Acetic Anhydride on Aluminosilicate Catalysts
摘要:
Reactions of epoxides prepared from alpha-, beta-pinenes and camphene with acetic anhydride on aluminosilicate catalysts (clay K-10, zeolite beta) were investigated affording various products of skeleton I C rearrangements: mono- and diacetates with five- and six-membered rings, and also with norbornane and pinane cores.